Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 0603-5063-21 recalled?

Perphenazine · 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0603-5063-21)

Yes — this exact package was recalled

1 FDA recall names the code 0603-5063-21 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
perphenazine
Strength
PERPHENAZINE 16 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Par Health USA, LLC
Type
Human Prescription Drug
Product code
0603-5063

Recalls naming this package

Class II ยท Moderate risk

Perphenazine

Labeling: Label Mixup: PERPHENAZINE, Tablet, 16 mg may have potentially been mislabeled as one of the following drugs: MELATONIN, Tablet, 1 mg, NDC 47469000466, Pedigree: AD46257_19, EXP: 5/15/2014; LITHIUM CARBONATE ER, Tablet, 450 mg, NDC 00054002025, Pedigree: AD60272_25, EXP: 5/22/2014; MONTELUKAST SODIUM, CHEW Tablet, 4 mg, NDC 00006071131, Pedigree: AD76639_11, EXP: 5/31/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-989-2014

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler